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Merck
CN

695572

Sigma-Aldrich

间碳硼烷-1-硫醇

96%

别名:

1,7-Dicarba-closo-dodecaborane-1-yl-thiol, 1,7-Dicarbadodecaborane(12)-1-thiol, 1-Mercapto-m-carborane

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关于此项目

经验公式(希尔记法):
C2H12B10S
化学文摘社编号:
分子量:
176.29
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
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方案

96%

表单

solid

mp

195-209 °C

SMILES字符串

SC12BBBBBBBBBC1B2

InChI

1S/C2H12B10S/c13-2-1(3-2)4-6-8-10-12-11-9-7-5-2/h1,3-13H

InChI key

IKKUVNFZJOSSLF-UHFFFAOYSA-N

一般描述

m-Carborane-1-thiol (M1) is a boron cluster compound that is also known as icosahedral carborane thiol. It forms a self-assembled monolayer (SAM) by attaching the thiol groups with surface atoms. This SAM forms a two dimensional matrix on the metal surface that enables the tuning of surface properties such as a work function, and wettability.

应用

M1 forms a mixed SAM with m-carborane-9-thiol (M9), which is used to tune the work function of gold and silver surfaces for the fabrication of organic light emitting diodes (OLEDs).

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mixed carboranethiol self-assembled monolayers on gold surfaces.
Yavuz A, et al.
Applied Surface Science, 413(1), 233-241 (2017)
?Carboranyl-cysteine??Synthesis, Structure and Self-Assembly Behavior of a Novel alpha-Amino Acid.
He T, et al.
Scientific Reports, 7(1), 16995-16995 (2017)
A coordination chemistry dichotomy for icosahedral carborane-based ligands.
Spokoyny AM, et al.
Nature Chemistry, 3(8), 590-590 (2011)
Kai Kristiansen et al.
ACS nano, 8(10), 10870-10877 (2014-10-08)
Strong and particularly long ranged (>100 nm) interaction forces between apposing hydrophobic lipid monolayers are now well understood in terms of a partial turnover of mobile lipid patches, giving rise to a correlated long-range electrostatic attraction. Here we describe similarly
Synthesis and properties of substituted icosahedral carborane thiols.
Plesek J and Stanislav H
Collection of Czechoslovak Chemical Communications, 46(3), 687-692 (1981)

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